A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521090



Internal ID20894451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:38591083..38591636hg38UCSC Ensembl
chr18:36171047..36171600hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38554
hg19554
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18040068
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521090
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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